Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor

Abstract The current paradigm of cancer medicine focuses on patient‐ and/or cancer‐specific treatments, which has led to continuous progress in the development of patient representatives (e.g., organoids) and cancer‐targeting carriers for drug screening. As breakthrough concepts, i) living cancer ti...

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Autores principales: Hyo‐Jin Yoon, Young Shin Chung, Yong Jae Lee, Seung Eun Yu, Sewoom Baek, Hye‐Seon Kim, Sang Wun Kim, Jung‐Yun Lee, Sunghoon Kim, Hak‐Joon Sung
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Publicado: Wiley 2021
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Acceso en línea:https://doaj.org/article/e8e6201eb435440cbaab6765c1b052e1
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spelling oai:doaj.org-article:e8e6201eb435440cbaab6765c1b052e12021-11-17T08:40:31ZCancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor2198-384410.1002/advs.202102640https://doaj.org/article/e8e6201eb435440cbaab6765c1b052e12021-11-01T00:00:00Zhttps://doi.org/10.1002/advs.202102640https://doaj.org/toc/2198-3844Abstract The current paradigm of cancer medicine focuses on patient‐ and/or cancer‐specific treatments, which has led to continuous progress in the development of patient representatives (e.g., organoids) and cancer‐targeting carriers for drug screening. As breakthrough concepts, i) living cancer tissues convey intact profiles of patient‐specific microenvironmental signatures. ii) The growth mechanisms of cancer mass with intense cell‐cell interactions can be harnessed to develop self‐homing nano‐targeting by using cancer cell‐derived nanovesicles (CaNVs). Hence, a tissueoid model of ovarian cancer (OC) is developed by culturing OC patient tissues in a 3D gel chip, whose microchannel networks enable perfusion to maintain tissue viability. A novel model of systemic cancer responses is approached by xenografting OC tissueoids into ischaemic hindlimbs in nude mice. CaNVs are produced to carry general chemotherapeutics or new drugs under pre/clinical studies that target the BRCA mutation or energy metabolism, thereby increasing the test scope. This pioneer study cross‐validates drug responses from the OC clinic, tissueoid, and animal model by demonstrating the alignment of results in drug type‐specific efficiency, BRCA mutation‐dependent drug efficiency, and metabolism inhibition‐based anti‐cancer effects. Hence, this study provides a directional foundation to accelerate the discovery of patient‐specific drugs with CaNV application towards future precision medicine.Hyo‐Jin YoonYoung Shin ChungYong Jae LeeSeung Eun YuSewoom BaekHye‐Seon KimSang Wun KimJung‐Yun LeeSunghoon KimHak‐Joon SungWileyarticlecancer cell‐derived nanovesiclesovarian cancerpatient‐specific treatmentsself‐homing nano‐targetingtissueoidScienceQENAdvanced Science, Vol 8, Iss 22, Pp n/a-n/a (2021)
institution DOAJ
collection DOAJ
language EN
topic cancer cell‐derived nanovesicles
ovarian cancer
patient‐specific treatments
self‐homing nano‐targeting
tissueoid
Science
Q
spellingShingle cancer cell‐derived nanovesicles
ovarian cancer
patient‐specific treatments
self‐homing nano‐targeting
tissueoid
Science
Q
Hyo‐Jin Yoon
Young Shin Chung
Yong Jae Lee
Seung Eun Yu
Sewoom Baek
Hye‐Seon Kim
Sang Wun Kim
Jung‐Yun Lee
Sunghoon Kim
Hak‐Joon Sung
Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
description Abstract The current paradigm of cancer medicine focuses on patient‐ and/or cancer‐specific treatments, which has led to continuous progress in the development of patient representatives (e.g., organoids) and cancer‐targeting carriers for drug screening. As breakthrough concepts, i) living cancer tissues convey intact profiles of patient‐specific microenvironmental signatures. ii) The growth mechanisms of cancer mass with intense cell‐cell interactions can be harnessed to develop self‐homing nano‐targeting by using cancer cell‐derived nanovesicles (CaNVs). Hence, a tissueoid model of ovarian cancer (OC) is developed by culturing OC patient tissues in a 3D gel chip, whose microchannel networks enable perfusion to maintain tissue viability. A novel model of systemic cancer responses is approached by xenografting OC tissueoids into ischaemic hindlimbs in nude mice. CaNVs are produced to carry general chemotherapeutics or new drugs under pre/clinical studies that target the BRCA mutation or energy metabolism, thereby increasing the test scope. This pioneer study cross‐validates drug responses from the OC clinic, tissueoid, and animal model by demonstrating the alignment of results in drug type‐specific efficiency, BRCA mutation‐dependent drug efficiency, and metabolism inhibition‐based anti‐cancer effects. Hence, this study provides a directional foundation to accelerate the discovery of patient‐specific drugs with CaNV application towards future precision medicine.
format article
author Hyo‐Jin Yoon
Young Shin Chung
Yong Jae Lee
Seung Eun Yu
Sewoom Baek
Hye‐Seon Kim
Sang Wun Kim
Jung‐Yun Lee
Sunghoon Kim
Hak‐Joon Sung
author_facet Hyo‐Jin Yoon
Young Shin Chung
Yong Jae Lee
Seung Eun Yu
Sewoom Baek
Hye‐Seon Kim
Sang Wun Kim
Jung‐Yun Lee
Sunghoon Kim
Hak‐Joon Sung
author_sort Hyo‐Jin Yoon
title Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
title_short Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
title_full Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
title_fullStr Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
title_full_unstemmed Cancer Patient Tissueoid with Self‐Homing Nano‐Targeting of Metabolic Inhibitor
title_sort cancer patient tissueoid with self‐homing nano‐targeting of metabolic inhibitor
publisher Wiley
publishDate 2021
url https://doaj.org/article/e8e6201eb435440cbaab6765c1b052e1
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